Title of Invention	USE OF TEA LEAF EXTRACT FOR INHIBITING MICROBIAL TRANSFORMANT
Abstract	The present invention relates to an efficient and cost effective use of preventing growth of genetic transformant bacteria Agrobacterium tumefaciens after transformation in plants by using tea leaf extract as a bactericide, wherein said use leads to elimination of common problem of polyphenol oxidation during transformation and thereby helps maintain regeneration potential in explants and also helps in increased transformation efficacy.

Title of Invention

USE OF TEA LEAF EXTRACT FOR INHIBITING MICROBIAL TRANSFORMANT

Abstract

The present invention relates to an efficient and cost effective use of preventing growth of genetic transformant bacteria Agrobacterium tumefaciens after transformation in plants by using tea leaf extract as a bactericide, wherein said use leads to elimination of common problem of polyphenol oxidation during transformation and thereby helps maintain regeneration potential in explants and also helps in increased transformation efficacy.

Full Text	USE OF TEA LEAF EXTRACT FOR INHIBITING MICROBIAL TRANSFORMANT Technical Field The present invention relates to using tea leaf extract as a bactericide for preventing growth of genetic transformant bacteria Agrobacterium tumefaciens after transformation in plants by wherein said use leads to elimination of common problem of polyphenol oxidation during transformation and thereby helps maintain regeneration potential in explants and also helps in increased transformation efficacy. Background Art Transgenics' appear to be the 'need of the hour' in view of the ever growing demand for quality crops all over the world (Somerville C.R. 1994. In: Production and Uses of Genetically Transformed Plants, Chapman and Hall, London (eds. Bevan M.W., Harrison R.D., Leaver C.J.). Transgenic production through genetic transformation of plants is brought about by introducing desired gene(s) from any living organism into the concerned plant by different methods of DNA delivery in order to impart different traits for crop improvement viz. disease and pest resistance, longer shelf life, better and added nutritional value, varied colours and scents, tolerance to abiotic stresses like drought, flood, cold, salt etc. Of the different methods of gene delivery into plants, the most popular and cost effective is producing transgenics through Agrobacterium tumefaciens. By this method explants that have the ability to regenerate into full grown plants under tissue culture conditions are infected with the disarmed and engineered strains of the soil bacteria 'Agrobacterium tumefaciens' containing the desired engineered genes. Once the infection has occurred, the virulence genes of the Agrobacterium tumefaciens gets triggered and this enables the bacterium to pass on the T-DNA containing the desired engineered gene into the plant cell/nucleus and finally the desired engineered gene gets integrated into the plant genome which then becomes genetically transformed. For successful and high frequency of genetic transformation of plants, fresh actively growing cultures of Agrobacterium tumefaciens containing the engineered and disarmed T-DNA is generally grown for 12-' at 25-30°C and 150-200 rpm in dark upto its log phase of growth when the ce; !ty becomes 1X109 cells/ml. The explants are then infected with these fresh cultures and allowed to incubate for a few days at optimal temperature and pH so that the T-DNA with the desired engineered gene is passed on to plant cell/nucleus which finally gets integrated into the plant genome. Once the gene is integrated either transiently or stably into plant genome, the residual Agrobacterium tumefaciens needs to be eliminated totally or else the residual Agrobacterium overgrows on the explant and prevents it from regenerating into a healthy plant and in severe cases even kills the explants. A serious drawback of Agrobacterium tumefaciens mediated genetic transformation protocols is the requirement of high cost and labour intensive steps of washing and subsequent repeated culturing of transformants onto a medium containing expensive bactericidal antibiotics in order to kill Agrobacterium tumefaciens. These repeated washings and sub-culture involving bactericidal antibiotics not only result in vitrification of the transformants but also in their loss due to severe bacterial overgrowth. The problem is so severe that about 50% of the transformants are lost due to bacterial overgrowth and many a times, the generally employed bactericidal antibiotics fail to prevent this loss at feasible doses. In a preliminary study, crude leaf extracts were found to have a bactericidal effect on the overgrowing Agrobacterium tumefaciens after co-cultivation, yet another important problem that was encountered was the loss and death of transformants due to phenol oxidation. It was therefore, necessary to optimize a concentration or composition of tea leaf extract that would not only kill the residual Agrobacterium tumefaciens after the transfer and integration of its T-DNA into the plant genome but would also overcome the problem of loss and death of the explants due to phenol oxidation. Tea leaves contain high levels of polyphenols which are composed of 6 types of catechins (C) and their derivatives viz., epicatechin (EC), gallocatechins (GC), epigallocatechins (EGC), epicatechin gallate (ECg), epigallocatechin gallate (EGCg). Besides polyphenols, tea leaves also contain caffeine, amino acids and other nitrogenous compounds, vitamins, inorganic elements, carbohydrates and lipids (Chu D-C and Juneja L.R. General chemical composition of green tea and its infusion. In: Chemistry and Application of Green Tea. 1997. CRC Press, N.York, eds. Yamamoto T., Juneja L.R., Chu D-C, Kim M.)- Tea polyphenols are known to show several biochemical activities suchas inhibition of bacterial mutation (Kada T., Kaneka K., Matsuzaki T. and Hara Y. 19bj. Detection and chemical identification of natural biomutagens. A case of green tea factor. Mutation Research 150: 127), inhibition of HIV reverse transcriptase activity (Nokane H. and Ono K. 1990. Differential inhibitory effects of some catechins derivatives on the activities of human immuno-deficiency virus reverse transcriptase and cellular deoxyribonucleic and ribonucleic acid polymerases. Biochemistry 29: 2841-5). Tea polyphenols have shown anticaries effects by inhibiting the adherence of P. gingivalis onto buccal epithelial cells at concentrations 250-500ng/ml which is much larger compared to the effective concentrations of antibiotics (Sakanaka S., Aizawa M., Kim M. and Yamamoto T. 1996 Inhibitory effects of green tea polyphenols on growth and cellular adherence of an oral bacterium Porphyromonal gingivalis. Biosci. Biotechnol. Biochem. 60: 745; Sakanaka S. 1997. Green tea polyphenols for prevention of dental caries In: Chemistry and Application of Green Tea. eds. Yamamoto T., Juneja L.R., Chu D-C, Kim M.). Tea polyphenols have also been reported to possess antiviral activity dependent on the galloyl moiety linked by ester linkage in catechin molecule (John T.J. and Mukundan P. 1979. Virus inhibition by tea, caffeine and tannic acid. Indian J. Med. Res. 69: 542; Nakayarna M., Toda ML, Okubo S. and Shimamura T. 1990. Inhibition of influenza virus infection by tea. Lett. Appl. Microbiol. 11: 38). Huang and Frankel, 1997 (Huang S-W and Frankel E.N. 1997 Antioxidant activity of tea catechins in different lipid systems. J. Agric. FoodChem. 45: 3033-8) have reported antioxidant activity of tea catechins in liposomes. Also tea catechins have been reported to scavenge the oxidative radicals that cause damage to the DNA (Yen G-W. and Chen H-Y. 1995. Antioxidant activity of various tea extracts in relation, to their antimutagenecity. J. Agric. Food Chem. 43: 27-32), and their oxygen radical absorbing action with antiproliferative action in human epidermoid carcinoma A431 cells (Lin Y-L., Juan I-M., Chen Y-L., Liang Y-C. and Lin J-K. 1996. Composition of polyphenols in fresh tea leaves and associations of their oxygen-radical-absorbing capacity with antiproliferative actions in fibroblast cells. J. Agric. Food Chem. 44: 1387-94). Saeki et al. 1999 (Saeki K., Sano M., Miyase T., Nakamura Y., Kara Y., Aoyagi Y. and Isemura M. Apoptosis-inducing activity of polyphenol compounds derived from tea catechins in human histiolytic lymphoma U937 cells. Biosci. Biotechnol. Biochem. 63: 585-7) have recorded the apoptosis inducing activity of polyphenols of tea as evidenced by inhibition of DNA ladder formation and chromatin condensation in human histolytic lymphoma cells. Antimicrobial activity of green tea extract has also been well documented at minimum inhibitory concentration or MIC (250\|ig/ml to lOOOng/ml) for several micro-organisms that are harmful to human health (In: Chemistry and Application of Green Tea. 1997. CRC Press, New York. eds. Yamamoto T., Juneja L.R., Chu D-C, Kim M.). Crude tea leaf extract thus, appears to be a potent agent for bactericidal formulations during genetic transformation, once the problem of phenolic oxidation and hence death of the transformants is alleviated. One of the problems encountered ^during plant tissue transformation with A. tumefaciens is the effective elimination of the bacterium after transfer of the transgenes has taken place. When using Agrobacterium as a tool in plant genetic engineering, there is a risk that if not all bacteria are eliminated after transformation, the residual bacteria will kill the transgenic plants. Therefore, strategies in genetic transformation generally require a balance between the bactericidal activity and the normal morphogenetic response of transformed tissue. Different reports on these problems include the report by Colby and Meredith (Colby S.M. and Meredith C. P. Kanamycin sensitivity of cultured tissues of Vitis Plant Cell Reports 9(5): 237-40) who used the bactericidal antibiotic carbenicillin for killing residual Agrobacterium tumefaciens during genetic transformation but the drawback of their report was that carbenicillin had inhibitory effects on plant regeneration which sometimes resembled those of growth inhibitors. Also, Park et al., 1990 (Park Y. G., Shin D.W., Kim J. H. 1990. Journal of Korean Forestry Society 79(3): 278-84) used a combination of cefotaxime (200 mg/litre) and carbenicillin (300 mg/litre) for Agrobacterium mediated transformation of Populus nigraXP. maximowiczii leaves. The drawback of the protocol was that although, the growth of Agrobacterium tumefaciens strain 6044 was reduced, yet, the residual Agrobacterium tumefaciens was not totally eliminated and the rate of regeneration was also as low as 10%. Yurkova et al., 1993 (Yurkova G. N., Chugunkova T. V. and Shevtsov I. A. 1993.. Effect of antibiotics on the tissue culture of sugarbeet and fodder beet. Tsitologiya-i-Genetika 27(2): 3-6) used a combination of claforan and carbenicillin as inhibitors of Agrobacterium cells during transformation of diploid sugarbeet hybrid and 2 diploid varieties of fodder beet. However, the drawback of this report was that this combination had an inhibiting effect on shoot formation. Yepes and Aldwinckle, 1994 (Yepes L. M. and Aldwinckle H. S. 1994. Micropropagation of thirteen Mains cultivars and rootstocks, and effect of antibiotics on proliferation. Plant Growth Regulation 15(1): 55-67) used cefotaxime at 200 mg/litre and carbenicillin at 500 mg/litre for the transformation of 13 apple cultivars. However, the drawback of the report was that while cefatoxime caused abnormal shoot morphology, carbenicillin alone or in combination with cefotaxime at 200 mg/litre, inhibited proliferation and caused excessive enlargement of the basal leaves, inducing callus formation and release of phenolic compounds in the medium.Linera/., 1995 (Lin-J J., Assad-GarciaN. andKuo, J. 1995. Plant hormone effect of antibiotics on the transformation efficiency of plant tissues by Agrobacterium tumefaciens cells. Plant Science Limerick. 109(2): 171-177) reported the use of 250 to 2000 ug/ml carbenicillin for the inhibition of bacterial (A. tumefaciens strains, LBA4404, C58 and EHA101) growth in tobacco leaf explants wherein they showed that LBA4404 was the most sensitive to carbenicillin and cefotaxime. However, the drawback of the protocol was that the regeneration efficiency from leaf explants decreased with the addition of increasing concentration of carbenicillin on MS medium containing 0.5 ug/ml of benzyladenine and/or 2,4-D wherein they emphasized on the toxic effects on leaf explants when grown on MS medium containing a combination of 250 ug/ml carbenicillin and 1 ug/ml 2,4-D due to the auxin related chemical structures of 2,4-D or NAA and carbenicillin. The major drawback of this protocol is that such plant growth regulators (2,4-D, BA or NAA) are generally used in most regeneration media that are employed for Agrobacterium tumefaciens mediated transformation. Sarma et al., 1995 (Sarma K.S., Evans N.E. and Selby C. 1995. Effect of carbenicillin and cefotaxime on somatic embryogenesis of Sitka spruce (Picea sitchensis (Bong.) Carr. Journal of Experimental Botany 46(292):, 1779-81) reported the use of antibiotics viz. carbenicillin and cefotaximethese in an attempt to transform Sitka spruce somatic embryos using Agrobacterium based vectors. They reported that carbenicillin should not be used for transformation of Sitka spruce. The drawback of the report was that carbenicillin prevented the development of mature somatic embryos, reduced early stage embryos by >90% and tissue growth by 50%. Cefotaxime had no effect on overall tissue growth, but reduced the development of early and mature embryos by 20% and 66-80%, respectively. Shackelford and Chlan 1996 (Shackelfofd > Chlan C.A. 1996. Identification of antibiotics that are effective in eliminating Agrobacterium tumefaciens. Plant Molecular Biology Reporter 14(1): 50-5) performed an assay using ten antibiotics viz. cefotaxime, carbenicillin, tfrythromycin, spectinomycin, polymixin B, chloramphenicol, methicillin, augmentin 500, augmentin 250 and moxalactam [latamoxef] inorder to identify the antibiotics that are most effective against A. tumefaciens strains EHA101 and LBA4404, and to determine if these antibiotics inhibited tobacco callus and shoot formation. This report indicates that a major drawback of most transformation protocol is time consuming assays involving several costly antibiotics for the effective elimination of A. tumefaciens after gene transfer into plant explant has taken place. Barrett et al., 1997 (Barrett C., Cobb E., McNicol.R. and Lyon G. 1997 A risk assessment study of plant genetic transformation using Agrobacterium and implications for analysis of transgenic plants. Plant Cell Tissue and Organ Culture. 47(2): 135-44) examined Agrobacterium transformation systems for Brassica, Solanum and Rubus, using carbenicillin, cefotaxime and ticaracillin [ticarcillin], respectively, to eliminate contamination, for the presence of residual Agrobacterium. Results indicated that none of the1 antibiotics tested succeeded in eliminating Agrobacterium and the contamination levels increased in explants from 12 to 16 weeks to such an extent that Solanum cultures senesced and died. This may be due to the fact that in some cases the minimum bactericidal concentration values (concentration to be used for elimination of contaminants in culture) for the three antibiotics were higher than the concentrations employed in the culture medium. Moreover, even up to 6 months after transformation, 50% of contaminated material still harboured bacterial cells with the binary vector at levels of 107 colony forming units per gram. This report indicates a major drawback with most of the generally used antibiotics are ineffective for Agrobacterium elimination in plants like Brassica, Solanum and Rubus and affects their regeneration as well as survival efficiency. Hammerschlag et al., 1997. (Hammerschlag F.A., Zimmerman R.H. Yadava, U.L., Hunsucker S. and Gercheva P. 1997. Effect of antibiotics and exposure to an acidified medium on the elimination of Agrobacterium tumefaciens from apple leaf explants and on shoot regeneration. Journal of the American Society for Horticultural Science. 122(6): 758-63) tested a range of antibiotics and their short-term exposure to an acidified (pH 3.0) medium for their effects on eliminating A. tu/t.^/aciens, supervirulent strain EHAld vp£HA101/pGT100), on leaf explam.. of Royal Gala apples (Malus domestica [M. pumila]) and on shoot regeneration. They reported that the exposure of leaf explants to regeneration and elongation media containing 100 (ag/ml of the antibiotics carbenicillin (crb), cefotaxime (cef), and cefoxitin (mefoxin (mef)), singly or in combination for 52 days, did not eliminate A. tumefaciens from the explants. The drawback of this report was that even short-term (I to 18-hour) vacuum infiltration with 500 ^g/rnl of any of the antibiotics did not inhibit regeneration and failed to completely eliminate A. tumefaciens from leaf explants. Cheng et al., 1998 (Cheng, Z. M., Schnurr, J. A. Kapaun, J. A. 1998.Timentin as an alternative antibiotic for suppression of Agrobacterium tumefaciens in genetic transformation. Plant Cell Reports 17(8): 646-9) studied the effects of timentin on shoot regeneration of tobacco (Nicotiana tabacum) and Siberian elm (Ulmus pumila) and its use for the suppression of Agrobacterium tumefaciens during genetic transformation. Timentinj - a mixture of ticarcillin and clavulanic acid was used effectively at concentrations of 200-500 mg/1 and at ratios of ticarcillinxlavulanic acid at 50:1 and 100:1. The drawback of this report is that although timentin is a less expensive alternative to the use of carbenicillin or cefotaxime antibiotics for the effective suppression of A. tumefaciens after genetic transformation yet it is expensive synthetic antibiotic as compared to natural agents like crude tea extracts. Ling et al., 1998 (Ling H.Q., Kriseleit D. and Ganal M.W. 1998. Effect of ticarcillin/potassium clavulanate on callus growth and shoot regeneration in Agrobacterium-mediated transformation of tomato (Lycopersicon esculentum Mill.) Plant Cell Reports 17(11): 843-7) studied the effect of Cefotaxime, ticarcillin/potassium clavulanate on tomato transformation. Cefotaxime did not inhibit callus growth in culture medium, but it clearly decreased shoot differentiation. While cefatoxime showed a strong negative effect on callus growth, shoot regeneration and transformation efficiency, the ticarcillin/potassium clavulanate was more economical and effective than carbenicillin and cefotaxime. The drawback of the report is that although ticarcillin/potassium clavulanate was a very good alternative to eliminate Agrobacteriurf tumefaciens in plant transformations yet it is an expensive synthetic antibiotic as compared to natural agents like crude tea extracts. Joersbo et al. 2000 (Joersbo M., Brunstedt, J. Marcussen, J. Okkels FT. 2000. Transformation of the endospermous legume guar (Cyamopsis tetragonoloba L.) and analysis of transgene transmission. Molecular-Breeding 5(6): 521-9) used carbenicillin and cefotaxime, for the elimination of Agrobacterium after co-culture, wherein they found considerable toxicity was displayed to guar tissues due to beta-lactams. When the beta-lactams were replaced by the non-phytotoxic beta-lactamase inhibitor usulbactam" alongwith thidiazuron and silver thiosulfate the problem was overcome. The drawback of this report was that while the commonly used carbenicillin and cefotaxime were phytotoxic to the explants used, replacement of beta-lactams by sulbactam is a costly process. Objects of the present invention The main object of the present invention is to develop a use of tea leaf extract for killing the overgrowth of AgrobactaGum tumefaciens in systems or plants or explants requiring longer co-cultivation periods in order to increase the transformation efficiency. Moreover, the crude tea extract is able to eliminate the risk of residual Agrobacterium released along with the transgenic plants thereby maintaining a balance between the selection pressures and the normal morphogenetic response. Another object of the present invention is the use of tea leaf extract for Agrobacterium tumefaciens genetic transformation in different systems or plants or explants wherein rhe generally used bactericidal antibiotics are ineffective. Further object of the present invention is to develop a use of tea leaf extract to enhance the transformation efficacy of the bacteria Agrobacterium tumefaciens. Another object of the present invention is to develop a use of tea leaf extract to enhance prevent polyphenol oxidation involved with such kind of transformation. Yet another object of the present invention is to develop use of tea leaf extract to enhance wherein normal growth of the transformed plant is not affected by the this mode of transformation involving bacteria Agrobacterium tumefaciens. Yet another object of the present invention is to develop a cost-effective system for Agrobacterium tumefaciens genetic transformation wherein no commercial and yet costly antibiotics are used. Still another object of the present invention is to develop an economical system for obtaining the bactericidal agent without involving any costly extraction methods wherein the crude leaf extract with bactericidal activity is extracted without requiring expensive instruments. Still another object of the invention is to develop a use of tea leaf extract wherein a crude leaf extract with bactericidal activity can be obtained in abundance from naturally growing tea bushes. Still another object of the present invention is to develop a use of tea leaf extract wherein the bactericidal agent is of natural origin and is not of synthetic or semi- synthetic nature. Still another object of present invention is to develop a use of tea leaf extract wherein, the bactericidal agent can be obtained in abundance from actively growing two and a bud making it economical. Still another object of the present invention is to develop a use of tea leaf extract t wherein, the bactericidal agent can be obtained in abundance from even the lower maintenance foliage thereby making it more economical as generally such leaves are discarded or burnt. Still another object of the present invention is to develop a use of tea leaf extract wherein, the crude leaf extract can also be used as a bactericidal agent for other contaminating bacteria in different in vitro systems involving different plants or explants. Still another object of the present invention is to develop a use of tea leaf extract wherein, the crude extract can also be used during 'hairy root production' using Agrobacterium rhizogenesis. . Still another object of the present invention is to develop use of tea leaf extract wherein.the transformation efficiency can be increased considerably by decreasing the mortality rate of transformants due to Agrobacterium overgrowth. Further object of the present invention is to obtain tea leaf extract having bactericidal property for Agrobacterium tumefaciens mediated genetic transformations which obviates the drawbacks as detailed above. Summary of the present invention The present invention relates to an efficient and cost effective use of tea leaf extract of preventing growth of genetic transformant bacteria Agrobacterium tumefaciens after transformation in plants by using tea leaf extract as a bactericide, wherein said use of tea leaf extract leads to elimination of common problem of polyphenol oxidation during transformation and thereby he'^ maintain regeneration potential in explan; ; and also helps in increased transforr efficacy. Detailed description of the present invention Accordingly, the present invention relates to an efficient and cost effective use of preventing growth of genetic transformant bacteria Agrobacterium tumefaciens after transformation in plants by using tea leaf extract as a bactericide, wherein said use leads to elimination of common problem of polyphenol oxidation during transformation and thereby helps maintain regeneration potential in explants and also helps in increased transformation efficacy. « In an embodiment of the present invention, use of tea leaf extract as a bactericide for preventing growth of genetic •transformant bacteria Agrobacterium tumefaciens after transformation in plants. In another embodiment of the present invention, inoculating said bacteria harbouring antibiotic resistant genes and reporter gus gene in a culture medium with said antibiotics. In yet another embodiment of the present invention, incubating the said culture in dark. In still another embodiment of the present invention, harvesting the ceils during log phase In still another embodiment of the present invention, pelleting live bacterial cells. In still another embodiment of the present invention, suspending the said pellet in fresh culture medium. In still another embodiment of the present invention, optimizing the cells density. In still another embodiment of the present invention, immersing various explants of different plants in bacterial suspension. In still another embodiment of the present invention, removing excess bacteria from explant. In still another embodiment of the present invention, incubating explant in media for different time durations. In still another embodiment of the present invention, preparing crude extract of tea leaf to be used as bactericide by drying leaves. In still another embodiment of the present invention, preparing acetone extract overnight. In • '!! another embodiment of the present ;nvention, filtering the extract. In still another embodiment of the present invention, extracting filterate with n-hexane to obtain aqueous and lipid layers. In still another embodiment of the present invention, concentrating aqueous layer to dryness. In still another embodiment of the present invention, diluting concentrated extract using with water to obtain crude tea extract. In still another embodiment of the present invention, estimating total catechins and caffeine in said extract. In still another embodiment of the present invention, transferring explants of various plants into medium containing various concentrations of 0-600 ug/ml of crude extract (figure 1) and catechin and caffeine fractions separately. In still another embodiment of the present invention, obtaining bacteria free • transgenic explants. 4 In still another embodiment of the present invention, wherein antibiotics are selected from a group comprising Kanamycin, and hygromycin. In still another embodiment of the present invention, wherein culture medium is yeast mannitol broth. In still another embodiment of trto present invention, wherein concentration of bacteria is ranging between 10.to 75 micrograms/ml. In still another embodiment of the present invention, wherein incubating culture at temperature ranging between 20 to 35° C. In still another embodiment of the present invention, wherein incubating culture at revolution rate ranging between 100 to 300 rpm for time duration ranging between 10 to 20 hours. In still another embodiment "of the present invention, wherein harvesting the said culture at optical density ranging between 0.6-0.8 at 600 nm for concentration of about 1 x 109 cells/ml. In still another embodiment of the present invention, wherein pelleting the harvest by centrifuging at 3000-9000 rpm for about 20 to 40 minutes. In still another embodiment of the present invention, wherein centrifuging said culture at temperature ranging between 20 to 35° C. In still another embodiment of the present invention, wherein cell density is measured spectrophotometrically. In still another embodiment of the present invention, wherein cell density is measured by estimating optical density after about every 6 hours interval to estimate growth rate of said bacteria spectrophotometrically. In still another embodiment of the present invention, wherein optimization of cell density has O.D. ranging between 0?6 to 0,8 at 600 nm at 1 X 109 cells/ml upto 60 hours. In still another embodiment of the present invention, wherein immersing said tea explant in bacterial suspension for time duration ranging between 3 to 40 minutes. In still another embodiment of the present invention, wherein removing excess bacteria from explant by blotting of explant on filter paper. In still another embodiment of the present invention, wherein co-cultivating explant for time duration ranging between 1 to 20 days. • In still another embodiment of the present invention, wherein concentration of tea * plant extract is ranging between 1 to 1000 mlcrograms/ml. In still another embodiment of the present invention, wherein leaves are dried in oven \at temperature ranging between 50 to 70° C. In still another embodiment of Jhe "present invention, wherein acetone is at concentration ranging between 5 to 50 %. In still another embodiment of the present invention, wherein acetone extract is prepared at room temperature. In still another embodiment of the present invention, wherein concentrating aqueous layer to drying using rotary evaporators. In still another embodiment of the present invention, wherein ratio of acetone and n- hexane is ranging between 4:5 to 12:1. In still another embodiment of the present invention, wherein concentration of tea leaf • extract in acetone solution is in the ratio ranging between 200 to 500 gms/L. In still another embodiment of the present invention, wherein concentration of catechins and caffeine is ranging between 2 to 750 micrograms/ml in culture. In still another embodiment of the present invention, wherein using tea extract as bactericide eliminates the problem of polyphenol oxidation. In still another embodiment of the present invention, wherein said plants show normal growth after using tea extract as bactericide. In still another embodiment of the present invention, wherein said use of tea leaf extract shows increased transformation efficacy. In still another embodiment of the- present invention, whcrein.the transformation efficiency can be increased considerably- by decreasing the mortality rate of transformants due to Agrobacterium overgrowth. In further embodiment of the present invention, the use of tea leaf extract of transformation used in the instant application employing bacteria Agrobacterium tumefaciens causes no polyphenol oxidation. The polyphenol oxidation usually affects the normal growth of the transformed plant in such kinds of transformation in plants. But, use of tea leaf extract as a bactericide after transformation of plant by said bacteria facilitate normal growth of the transformed plant. In another embodiment of the present invention, transformation efficacy facilitated by the said bacteria rises on the use of tea leaf extract as a bactericide for Agrobacterium tumefaciens. The said extract decreases the mortality rate of transformant due to bacterial overgrowth. In further embodiment of the present Jinvention, tea leaf extract as a potent bactericidal agent for Agrobacterium tumefaciens mediated genetic transformations which comprises (i) inoculation of two strains of Agrobacterium tumefaciens viz. EHA105 (mild) and GV2260 (virulent) harbouring the antibiotic resistance genes for kanamycin or hygromycin and the reporter gus gene from mother cultures of respective strains into 10-30 ml liquid modified Yeast Mannitol Broth with kanamycin or hygromycin (ii) incubation for 12-16 hr at 25-30°C and 150-200 rpm in dark (iii) harvesting at 0.6-0.8 optical density at 600 nm for lX109cells/ml during log phase of bacterial growth (iv) pelleting of living bacterial cells by centrifugation at 15-30 minutes at 4000-8000 rpm and 25-30°C (v) suspension of bacterial pellet in fresh 5-25ml of Yeast Mannitol Broth without damaging the bacterial cells (vi) optimization of bacterial cell density at lX109cells/ml by measuring optical density at 600 nm (vii) immersion of various explants of different plants in bacterial suspension for 5-35 minutes (viii) blotting of explants on filter papers to remove excess Agrobacterium tumefaciens (ix) incubation of explants on incubation medium for different periods of 1-10 days (x) preparation of crude extract of tea leaf to be used as a bactericidal agent by drying 100-500g fresh tea leaves of Kangra jat in an oven at 60°C (xi) overnight extraction of dried leaves at room temperature with 0.4-1.2 liters of 10-40 ueous acetone and filteration (xii) extraction of the filtrate with 100-500 ml nexane to obtain two layers for removal of lipids (xiii) the aqueous layer taken and concentrated to dryness using standard rotary evaporators (xiv) concentrated extract diluted with water to 10-50 ml and total catechins and caffeine estimated (xv) the aqueous extract served as a crude mixture (xvi) transfer of various explants of different plants to regeneration medium containing different concentrations of 0-600u.g/ml crude tea extract and catechin and caffeine fractions separately for totally killing the residual Agrobacterium tumefaciens and for eliminating the problem of polyphenol oxidation in the explants in order to maintain the regeneration potential of explants (xi) transfer of Agrobacterium tumefaciens free explants to regeneration medium containing selection antibiotics for further regeneration and transgenic plant development (xii) optimization of the concentration and fractions of tea leaf extract on the growth curve of Agrobacterium tumefaciens in both solid and liquid Yeast Mannitol Broth media in order to determine the optimum concentration for desired bactericidal activity as well as for promoting regeneration potential of the explant. In further embodiment of the present invention, different explants of different plant species were used for transgenic production. In yet another embodiment of the present invention, different concentrations of filter • sterilized and autoclaved de-caffeinated fractions of catechin were added as above. In still another embodiment of the present invention, different concentrations of D-catechin of Acacia species were used as mentioned above wherein D-catechin was found to promote and not inhibit the growth of Agrobacterium tumefaciens. In still another embodiment of the present-invention, since green tea extract is known to have antimicrobial activity against several micro-organisms that are harmful to human health at minimum inhibitory concentration or MIC at 250\|ig/ml to 1000u.g/ml, it was presumed that crude leaf extract could be used to kill overgrowing Agrobacterium tumefaciens during genetic transformation. In still another embodiment of the present invention, this property of crude leaf extract can be successfully employed to overcome the serious problems of Agrobacterium tumefaciens overgrowth and also in preventing the loss of the transformants due to ineffective bactericidal antibiotics such as carbenicillin, cefatoxime, tricaricillin that are generally used in genetic transformation experiments in order to kill overgrowing Agrobacterium tumefaciens. Use of crude tea leaf extract for genetic transformation in plants not only has the potential of providing abundantly available natural source of bactericidal agent but is aiso effective in cutting down the cost of commercially used antibiotics. Moreover, since the crude extracts are also obtained from the maintenance foliage leaves that are generally discarded and burnt, this use of tea leaf extract appears to be all the more economical and cost effective. Use of crude tea leaf extract is specially important in increasing the transformation efficiency because even the explants or plant species requiring long periods of co-cultivation can be recovered by killing the Agrobacterium tumefaciens. In still another embodiment of the present invention, different explants like leaf, somatic embryo, callus and zygotic axes of tea were used using crude leaf extract of tea cultivars assamica and chinary instead "of generally used antibiotics for transgenic production following the use of tea leaf extract outlined in Example. In still another embodiment of the present invention, different explants of different plant species like carnation and rose leaf, somatic embryo, callus were used during genetic transformation using crude leaf extract following the use of tea leaf extracts outlined in Example 1. In still another embodiment of the present invention, different concentrations of filter sterilized and autoclaved de-caffeinated fractions of catechin were added as above for the production of transgenics instead of generally used antibiotics like carbenicillin, cefatoxime, tricaricillin etc. following the use of tea leaf extracts outlined in example 1. In still another embodiment of the present invention, different concentrations of D-catechin of Acacia species were used as mentioned above instead of generally used antibiotics like carbenicillin, cefatoxime, tricaricillin wherein D-catechin was found to promote and not inhibit the growth of Agrobacterium tumefaciens. In further embodiment of the present invention, applicant has claimed an extract as a potent bactericidal agent for Agrobacterium tumefaciens mediated genetic transformations comprising of steps (i) inoculation of two strains of Agrobacterium tumefaciens viz. EH A105 (mild) and GV2260 (virulent) harbouring the antibiotic resistance genes for kanamycin or hygromycin and the reporter gus gene from mother cultures of respective strains into 10-30 ml liquid modified Yeast Mannitol Broth with kanamycin or hygromycin (ii) incubation for 12-16 hr at 25-30°C and 150-200 rpm in dark (Hi) harvesting at 0.6-0.8 optical density at 600 nm for lX109cells/ml during log phase of bacterial growth (iv) pelleting of living bacterial cells by centrirugation at 15-30 minutes at 4000-8000 rpm and 25-30°C (v) suspension of bacterial pellet in fresh 5-25ml of Yeast Mannitol Broth without damaging the bacterial cells (vi) optimization of bacterial cell density at lX109cells/ml by measuring optical density at 600 nm (vii) immersion of various explants of different plants in bacterial suspension for 5-35 minutes (viii) blotting of explants on filter papers to remove excess Agrobacterium tumefaciens (ix) incubation of explants on incubation medium for different periods of 1-10 days (x) preparation of crude extract of tea leaf to be used as a bactericidal agent by drying 100-500g fresh tea leaves of Kangra jat in an oven at 60°C (xi) overnight extraction of dried leaves at room temperature with 0.4-1.2 liters of 10-40% aqueous acetone and filteration (xii) extraction of the filtrate with 100-500 ml of n-hexane to obtain two layers for removal of lipids (xiii) the aqueous layer taken and concentrated to dryness using standard rotary evaporators (xiv) concentrated extract diluted with water to 10-50 ml and total catechins and caffeine estimated (xv) the aqueous extract served as a crude mixture (xvi) transfer of various explants of different plants to regeneration medium containing different concentrations of 0-600\|ig/ml crude tea extract and catechin and caffeine fractions separately for totally killing the residual Agrobacterium tumefaciens and for eliminating the problem of polyphenol oxidation in the explants in order to maintain the regeneration potential of explants (xvii) transfer of Agrobacterium tumefaciens free explants to regeneration medium containing selection antibiotics for further regeneration and transgenic plant development (xviii) optimization of the concentration and fractions of tea leaf extract on the growth curve of Agrobacterium tumefaciens in both solid and liquid Yeast Mannitol Broth media in order to determine the optimum concentration for desired bactericidal activity as well as for promoting regeneration potential of the explant. In still another embodiment of the present invention, wherein two strains of Agrobacterium tumefaciens viz. EHA105 (mild) and GV2260 (virulent) harbouring the antibiotic resistance genes for kanamycin or hygromycin and the reporter gus gene from mother cultures of respective strains were inoculated into 10-30 ml liquid modified Yeast Mannitol Broth with "kanamycin or hygromycin. In still another embodiment of the present invention, wherein the above Agrobacterium tumefaciens cultures were harvested at 0.6-0.8 optical density at 600 nm for lX109cells/ml during log phase of bacterial growth. In still another embodiment of the jjrtsent invention, wherein bacterial pellet was suspended in fresh 5-25ml of Yeast Mannitol Broth without damaging the bacterial cells. In still another embodiment of the present invention, wherein bacterial cell density was optimized at 1XI 09cells/ml by measuring optical density at 600 nm. In still another embodiment of the present invention, wherein dried leaves overnight extracted at room temperature with 0.4-1.2 liters of 10-40% aqueous acetone and filtered and the filtrate extracted with 100-500 ml of n-hexane to obtain two layers for removal of lipids. In still another embodiment of the present invention, wherein concentrated extract was diluted with water to 10-50 ml and total catechins and caffeine estimated. In still another embodiment of the present invention, wherein the aqueous extract served as a crude mixture. In still another embodiment of the present invention, wherein various explants of different plants were transferred to regeneration medium containing different concentrations of 0-600ng/ml crude tea extract and catechin and caffeine fractions separately for totally killing the .residual Agrobacterium tumefaciens and for eliminating the problem of polyphenol oxidation in the explants in order to maintain the regeneration potential of explants the cultures containing crude tea leaf extract were maintained at 25-30°C.in dark at 150-200 rpm for 48 hr. In still another embodiment of the present invention, wherein the crude leaf extract having bactericidal properties can be obtained in abundance from even the lower maintenance foliage thereby making it more economical as generally such leaves are discarded or burnt. In still another embodiment of the present invention, wherein the crude leaf extract can also be used as a bactericidal agent for other contaminating bacteria in different in vitro systems involving different plants or explants. In still another embodiment of the present invention, wherein the crude leaf extract can be used to increase the transformation efficiency considerably by decreasing the mortality rate of transformants due to Agrobacterium overgrowth. BRIEF DESCRIPTION OF THE ACCOMPANYING DRAWING Fig.l shows spectrophotometric decrease in absorbance with increasing concentration of crude leaf extracts. The' concentration of crude leaf extract is ranging between l-400\|ag/ml. The following examples are given by way of illustration and therefore should not be • construed to limit the scope of the present jnvention. EXAMPLE-1 Two strains of Agrobacterium tumefdctens viz. ERA 105 (mild) and GV2260 (virulent) harbouring the antibiotic resistance genes for kanamycin or hygromycin **•• and the reporter gus gene were inoculated froni mother cultures of respective strains into 10-30 ml liquid modified Yeast Mannitol Broth with kanamycin or hygromycin. The cultures were incubated for 12-16 hr at 25-30°C and 150-200 rpm in dark and harvested at 0.6-0.8 optical density at 600 nm for lX109cells/ml during log phase of bacterial growth. The living bacterial cells were pelleted by centrifugation at 15-30 minutes at 4000-8000 rpm and 25-30°C and suspended in fresh 5-25ml of Yeast Mannitol Broth without damaging the bacterial cells. The bacterial cell density at lX109cells/mi was optimized by measuring optical density at 600 nm. Various explants of different plants were immersed in bacterial suspension for 5-35 minutes and blotted on filter papers to remove excess Agrobacterium tumefaciens. The explants were incubated on incubation medium for different periods of 1-10 days. Crude extract of tea leaf was prepared to be used as a bactericidal agent by drying 100-500g fresh tea leaves of Kangra jat in an oven at 60°C. Dried leaves were extracted overnight at room temperature with 0.4-1.2 liters of 10-40% aqueous acetone and filtered. The filtrate extracted with 100-500 ml of n-hexane to obtain two layers for removing lipids and the aqueous layer concentrated to dryness using standard rotary evaporators and diluted with water to 10-50 ml. Total catechins and caffeine estimated and the aqueous extract served as a crude mixture. Various explants of different plants were transferred to regeneration medium containing different concentrations of 0-600ng/ml crude tea extract for totally killing the residual Agrobacterium tumefaciens and for eliminating the pr, em of polyphenol oxidation in the e ints in order to maintain the regener >n potential of explants. The Agrobacterium tumefaciew free 'explants were transferred to regeneration medium containing kanamycin or hygromycin for further regeneration and transgenic plant development. Concentrations and fractions of tea leaf extract were tested on the growth curve of Agrobacterium tumefaciens in both solid and liquid Yeast Mannitol Broth media in order to determine the optimum concentration for desired bactericidal activity as well as for promoting regeneration potential of the explant. EXAMPLE-2 Two strains of Agrobacterium tumefaciens viz. EHA105 (mild) and GV2260 (virulent) harbouring the antibiotic resistance genes for kanamycin or hygromycin and the reporter gus gene were inoculated from mother cultures of respective strains into 10-30 ml liquid modified Yeast Mannitol Broth with kanamycin or hygromycin. The cultures were incubated for 12-16 hr at 25-30°C and 150-200 rpm in dark and harvested at 0.6-0.8 optical density at 600 nm for lX109cells/ml during log phase of bacterial growth. The living bacterial cells were pelleted by centrifugation at 15-30 minutes at 4000-J8000 rpm and 25-30°C and suspended in fresh 5-25ml of Yeast Mannitol Broth without damaging the bacterial cells. Measurement of optical density at 600 nm at regular 6hr intervals for 0-48 hr and the mean ot ihree readings were plotted for development of the growth curve. Crude mixture of catechins as well as caffeine at concentrations of 2-600ug/ml were added to fresh cultures of Agnobacterium tumefaciens and maintained at 25-30°C in dark at 150-200 rpm for 48 hr. The optical density was again measured at regular interval of 6 hr each for 0-48hr for the plotting of the mean of the three readings in a linear graph in order to determine the effect of the crude mixture of catechins as well as caffeine at concentrations of 2-600ng/ml on fresh cultures of Agrobacterium tumefaciens (Fig. 1). EXAMPLE-3 Single colony of Agrobacterium tumefaciens was streaked on agar solidified plates containing different concentrations 2-600jj,g/ml of crude tea leaf extract containing mixture of catechins and caffeine in order to determine its bactericidal effect on agar solidified media by incubating'the plates at 25-30°C in dark for 12-16 hr. Advantages of the present invention: 1. The main advantage of the present invention is that its an efficient and cost effective use of tea leaf extract of preventing growth of genetic transformant bacteria Agrobacteriwn tumefaciens after transformation in plants by using tea leaf extract as a bactericide. 2. Another advantage of the instant application is that it's a use of tea leaf extract for enhanced genetic transformation in plant systems using bacteria Agrobacterium tumefaciens as the transformant. 3. Yet another advantage of the present invention is that it's a use of tea leaf extract for prevention of overgrowth of genetic transformant of plants wherein the growth of the plant after transformation is normal with no polyphenol oxidation. 4. Still another advantage is a use of tea leaf extract wherein, crude tea leaf extract can be used as a potent bactericidal agent for Agrobacterium tumefaciens mediated genetic transformations as it can be used for killing the overgrowth of Agrobacterium tumefaciens in systems or plants or explants requiring longer co- cultivation periods thereby increasing the transformation efficiency. 5. Still another advantage is a use of tea 4eaf extract wherein, crude tea leaf extract can be used for Agrobacterium tumefuCiens mediated genetic transformation in different systems or plants or explants jvherein the generally used bactericidal antibiotics are ineffective. v 6. Still another advantage is a use of tea leaf extract wherein, since no commercial bactericidal antibiotics need to be used, crude tea leaf extract prove to be a cost effective system for Agrobacterium tumefaciens mediated genetic transformation. 7. Still another advantage is a use of tea leaf extract wherein, since the crude leaf extract with bactericidal activity is obtained without involving any expensive instruments or costly extraction use of tea leaf extracts, its use proves to be an economical use of tea leaf extract. 8. Still another advantage is a use of tea leaf extract wherein, the crude leaf extract with bactericidal activity can be easily obtained in abundance from naturally growing tea bushes round the year. 9. Still another advantage is a use of tea leaf extract wherein, the crude leaf extract as a bactericidal agent is of natural origin and is not of synthetic or semi- synthetic nature. 10. Still another advantage is a use of tea leaf extract wherein, the crude leaf extract as a bactericidal agent can be obtained in abundance from even the lower maintenance foliage thereby making it more economical as generally such leaves are discarded or burnt. 11. Still another advantage is a use of tea leaf extract \vherein5 the crude leaf extract can also be used as a bactericidal agent for other contaminating bacteria in different in vitro systems involving different plants or explants. 12. Still another advantage is a use of tea leaf extract wherein, the crude tea leaf extract can also be used during 'hairy root production' using Agrobacterium rhizogenesis. 13. Still another advantage is a use of tea leaf extract wherein, the crude leaf extract can be used to increase the transformation efficiency considerably by decreasing the mortality rate of transformants due to Agrobacterium overgrowth. We Claim: 1. A method of inhibiting growth of genetic transformant bacteria Agrobacterium tumefaciens after transformation in plants selected from the group consisting of tea, carnations, and roses, said method comprising: (1) inoculating Agrobacterium tumefaciens bacteria strains EHA105 and GV2260 harbouring antibiotic resistant genes for kanamycin and/or hygromycin and a reporter gus gene from mother cultures of said respective strains into a liquid-modified yeast mannitol broth with kanamycin and/or hygromycin, thereby forming a culture comprising said bacteria at a concentration of from 10 to 75 micrograms/ml; (2) incubating the culture in darkness for a time duration of 10 20 hours at a temperature of 20 35.degree. C. and at a revolution rate of 100 300 rpm; (3) after said incubation, harvesting the culture at 0.6 0.8 optical density at 600 nm for concentration of 1.times. lO.sup.9 cells/ml during log phase of bacterial growth; (4) pelleting live bacterial cells in the harvested culture by centrifuging the harvested culture for a time duration of 15 40 minutes at a revolution rate of 3000 9000 rpm and at a temperature of 20 35.degree. C, thereby forming a pellet; (5) suspending the pellet in a fresh yeast mannitol broth medium to form a bacterial suspension; (6) optimizing bacterial cell density at 1.times. lO.sup.9 cells/ml of the bacterial suspension by measuring optical density at 600 nm after about every 6 hours interval to estimate growth rate of the bacteria spectrophotometrically, wherein optimization of cell density has an optical density ranging between 0.6 and 0.8 at 600 nm at l.times. 10. sup. 9 cells/ml; (7) immersing one or more explants of one or more plants in the bacterial suspension for a time duration of from 3 to 40 minutes, the explants being selected from the group consisting of leaf, somatic embryo, callus and zygotic axes; (8) removing excess genetic transformant Agrobacterium tumefaciens bacteria from said one or more explants; (9) incubating the explants obtained in step (8) in an incubation medium for a time duration of from 1 to 20 days; (10) preparing a crude extract of tea by a process comprising: (a) drying fresh tea leaves of Kangra jat in an oven at a temperature of from 50.degree. C. to 700.degree. C; (b) combining the dried fresh tea leaves with a 10 40% aqueous acetone to form a leaves/acetone solution and subjecting said dried fresh tea leaves to overnight extraction at room temperature with the aqueous acetone to form an extract, the dried fresh leaves being present in the leaves/acetone solution at a concentration of from 200 to 500 grams/liter, and the acetone being present in the leaves/acetone solution at a concentration of from 5 to 50%; (c) filtering the extract to form a filtrate; (d) extracting the filtrate with n-hexane to obtain an aqueous layer and a lipid layer; the ratio of acetone or n-hexane during extraction being from 4:5 to 12:1; (e) concentrating the aqueous layer to dryness; and (f) diluting the concentrated aqueous layer with water to obtain said crude tea extract, the crude tea extract comprising catechins and caffeine at a concentration of from 2 to 750 micrograms/ml; (11) characterised in that the one or more explants as obtained in step (9) are transferred to a regeneration medium containing from 1 to 1000 micrograms/ml of the crude tea extract prepared in step (10); and (12) maintaining the one or more explants in said regeneration medium in darkness at 25 30.degree. C. at 150 200 rpm for 48 hours, thereby obtaining one or more explants upon which growth of genetic transformant bacteria Agrobacterium tumefaciens is inhibited. 2. A method as claimed in claim 1, wherein said tea extract eliminates polyphenol oxidation during transformation. 3. A method as claimed in claim 1, wherein said one or more explants show normal growth after incubation with said crude tea extract in step (12). 4.A method as claimed in claim 1, wherein cell density is measured spectrophotometrically. 5. A method as claimed in claim 1, wherein in step (8) said excess genetic transformant Agrobacterium tumefaciens bacteria is removed from said one or more explants by blotting said one or more explants on filter paper. 6. A method as claimed in claim 1, wherein in step (10)(a), the fresh tea leaves are dried in an oven at a temperature of 60.degree. C. 7. A method as claimed in claim 1, wherein in step (10)(e), said aqueous layer is concentrated to dryness using rotary evaporators. 8. A method as claimed in claim 1, wherein in step (2), said culture is incubated for a time duration of 12 16 hours at a temperature of 25 30.degree. C. and at a revolution rate of 150-200 rpm. 9. A method as claimed in claim 1, wherein in step (4), the harvest is pelleted by centrifuging at 4000 8000 rpm for a time duration of 15 to 30 minutes and at a temperature of 25-30.degree. C. 10. A method as claimed in claim 1, wherein said culture is centrifuged at a temperature ranging between 25 to 30.degree. C. 11. A method as claimed in claim 1, wherein in step (7), the one or more explants are immersed in the bacterial suspension for a time duration of from 5 to 35 minutes. 12. A method as claimed in claim 1, wherein in step (10)(b), the dried fresh tea leaves are combined with from 0.4 to 1.2 liters of the aqueous acetone. 13. A method as claimed in claim 1, wherein in step (10)(d), the filtrate is extracted with 100-500 ml of the n-hexane. 14. A method as claimed in claim 1, wherein in step (10)(f), the concentrated aqueous layer is diluted with water to 10-50 ml.

Full Text

USE OF TEA LEAF EXTRACT FOR INHIBITING MICROBIAL TRANSFORMANT
Technical Field
The present invention relates to using tea leaf extract as a bactericide for preventing
growth of genetic transformant bacteria Agrobacterium tumefaciens after transformation in plants by wherein said use leads to elimination of common problem of polyphenol oxidation during transformation and thereby helps maintain
regeneration potential in explants and also helps in increased transformation efficacy.
Background Art
Transgenics' appear to be the 'need of the hour' in view of the ever growing demand
for quality crops all over the world (Somerville C.R. 1994. In: Production and Uses of Genetically Transformed Plants, Chapman and Hall, London (eds. Bevan M.W., Harrison R.D., Leaver C.J.).
Transgenic production through genetic transformation of plants is brought about by introducing desired gene(s) from any living organism into the concerned plant by different methods of DNA delivery in order to impart different traits for crop improvement viz. disease and pest resistance, longer shelf life, better and added nutritional value, varied colours and scents, tolerance to abiotic stresses like drought, flood, cold, salt etc.
Of the different methods of gene delivery into plants, the most popular and cost effective is producing transgenics through Agrobacterium tumefaciens. By this method explants that have the ability to regenerate into full grown plants under tissue culture conditions are infected with the disarmed and engineered strains of the soil bacteria 'Agrobacterium tumefaciens' containing the desired engineered genes. Once the infection has occurred, the virulence genes of the Agrobacterium tumefaciens gets triggered and this enables the bacterium to pass on the T-DNA containing the desired engineered gene into the plant cell/nucleus and finally the desired engineered gene gets integrated into the plant genome which then becomes genetically transformed.
For successful and high frequency of genetic transformation of plants, fresh actively growing cultures of Agrobacterium tumefaciens containing the engineered and disarmed T-DNA is generally grown for 12-' at 25-30°C and 150-200 rpm in dark upto its log phase of growth when the ce; !ty becomes 1X109 cells/ml. The explants are then infected with these fresh cultures and allowed to incubate for a few

days at optimal temperature and pH so that the T-DNA with the desired engineered gene is passed on to plant cell/nucleus which finally gets integrated into the plant genome. Once the gene is integrated either transiently or stably into plant genome, the residual Agrobacterium tumefaciens needs to be eliminated totally or else the residual Agrobacterium overgrows on the explant and prevents it from regenerating into a healthy plant and in severe cases even kills the explants. A serious drawback of Agrobacterium tumefaciens mediated genetic transformation protocols is the requirement of high cost and labour intensive steps of washing and subsequent repeated culturing of transformants onto a medium containing expensive bactericidal antibiotics in order to kill Agrobacterium tumefaciens. These repeated washings and sub-culture involving bactericidal antibiotics not only result in vitrification of the transformants but also in their loss due to severe bacterial overgrowth. The problem is so severe that about 50% of the transformants are lost due to bacterial overgrowth and many a times, the generally employed bactericidal antibiotics fail to prevent this loss at feasible doses.
In a preliminary study, crude leaf extracts were found to have a bactericidal effect on the overgrowing Agrobacterium tumefaciens after co-cultivation, yet another important problem that was encountered was the loss and death of transformants due to phenol oxidation. It was therefore, necessary to optimize a concentration or composition of tea leaf extract that would not only kill the residual Agrobacterium tumefaciens after the transfer and integration of its T-DNA into the plant genome but would also overcome the problem of loss and death of the explants due to phenol oxidation.
Tea leaves contain high levels of polyphenols which are composed of 6 types of catechins (C) and their derivatives viz., epicatechin (EC), gallocatechins (GC), epigallocatechins (EGC), epicatechin gallate (ECg), epigallocatechin gallate (EGCg). Besides polyphenols, tea leaves also contain caffeine, amino acids and other nitrogenous compounds, vitamins, inorganic elements, carbohydrates and lipids (Chu D-C and Juneja L.R. General chemical composition of green tea and its infusion. In: Chemistry and Application of Green Tea. 1997. CRC Press, N.York, eds. Yamamoto T., Juneja L.R., Chu D-C, Kim M.)- Tea polyphenols are known to show several biochemical activities such*as inhibition of bacterial mutation (Kada T., Kaneka K., Matsuzaki T. and Hara Y. 19bj. Detection and chemical identification of natural biomutagens. A case of green tea factor. Mutation Research 150: 127),

inhibition of HIV reverse transcriptase activity (Nokane H. and Ono K. 1990. Differential inhibitory effects of some catechins derivatives on the activities of human immuno-deficiency virus reverse transcriptase and cellular deoxyribonucleic and ribonucleic acid polymerases. Biochemistry 29: 2841-5). Tea polyphenols have shown anticaries effects by inhibiting the adherence of P. gingivalis onto buccal epithelial cells at concentrations 250-500ng/ml which is much larger compared to the effective concentrations of antibiotics (Sakanaka S., Aizawa M., Kim M. and Yamamoto T. 1996 Inhibitory effects of green tea polyphenols on growth and cellular adherence of an oral bacterium Porphyromonal gingivalis. Biosci. Biotechnol. Biochem. 60: 745; Sakanaka S. 1997. Green tea polyphenols for prevention of dental caries In: Chemistry and Application of Green Tea. eds. Yamamoto T., Juneja L.R., Chu D-C, Kim M.). Tea polyphenols have also been reported to possess antiviral activity dependent on the galloyl moiety linked by ester linkage in catechin molecule (John T.J. and Mukundan P. 1979.
Virus inhibition by tea, caffeine and tannic acid. Indian J. Med. Res. 69: 542; Nakayarna M., Toda ML, Okubo S. and Shimamura T. 1990. Inhibition of influenza virus infection by tea. Lett. Appl. Microbiol. 11: 38). Huang and Frankel, 1997 (Huang S-W and Frankel E.N. 1997 Antioxidant activity of tea catechins in different lipid systems. J. Agric. FoodChem. 45: 3033-8) have reported antioxidant activity of tea catechins in liposomes. Also tea catechins have been reported to scavenge the oxidative radicals that cause damage to the DNA (Yen G-W. and Chen H-Y. 1995. Antioxidant activity of various tea extracts in relation, to their antimutagenecity. J. Agric. Food Chem. 43: 27-32), and their oxygen radical absorbing action with antiproliferative action in human epidermoid carcinoma A431 cells (Lin Y-L., Juan I-M., Chen Y-L., Liang Y-C. and Lin J-K. 1996. Composition of polyphenols in fresh tea leaves and associations of their oxygen-radical-absorbing capacity with antiproliferative actions in fibroblast cells. J. Agric. Food Chem. 44: 1387-94). Saeki et al. 1999 (Saeki K., Sano M., Miyase T., Nakamura Y., Kara Y., Aoyagi Y. and Isemura M. Apoptosis-inducing activity of polyphenol compounds derived from tea catechins in human histiolytic lymphoma U937 cells. Biosci. Biotechnol. Biochem. 63: 585-7) have recorded the apoptosis inducing activity of polyphenols of tea as evidenced by inhibition of DNA ladder formation and chromatin condensation in human histolytic lymphoma cells. Antimicrobial activity of green tea extract has

also been well documented at minimum inhibitory concentration or MIC (250|ig/ml to lOOOng/ml) for several micro-organisms that are harmful to human health (In: Chemistry and Application of Green Tea. 1997. CRC Press, New York. eds. Yamamoto T., Juneja L.R., Chu D-C, Kim M.). Crude tea leaf extract thus, appears to be a potent agent* for bactericidal formulations during genetic transformation, once the problem of phenolic oxidation and hence death of the transformants is alleviated.
One of the problems encountered ^during plant tissue transformation with A. tumefaciens is the effective elimination of the bacterium after transfer of the transgenes has taken place. When using Agrobacterium as a tool in plant genetic engineering, there is a risk that if not all bacteria are eliminated after transformation, the residual bacteria will kill the transgenic plants. Therefore, strategies in genetic transformation generally require a balance between the bactericidal activity and the normal morphogenetic response of transformed tissue. Different reports on these problems include the report by Colby and Meredith (Colby S.M. and Meredith C. P. Kanamycin sensitivity of cultured tissues of Vitis Plant Cell Reports 9(5): 237-40) who used the bactericidal antibiotic carbenicillin for killing residual Agrobacterium tumefaciens during genetic transformation but the drawback of their report was that carbenicillin had inhibitory effects on plant regeneration which sometimes resembled those of growth inhibitors.
Also, Park et al., 1990 (Park Y. G., Shin D.W., Kim J. H. 1990. Journal of Korean Forestry Society 79(3): 278-84) used a combination of cefotaxime (200 mg/litre) and carbenicillin (300 mg/litre) for Agrobacterium mediated transformation of Populus nigraXP. maximowiczii leaves. The drawback of the protocol was that although, the growth of Agrobacterium tumefaciens strain 6044 was reduced, yet, the residual Agrobacterium tumefaciens was not totally eliminated and the rate of regeneration was also as low as 10%.
Yurkova et al., 1993 (Yurkova G. N., Chugunkova T. V. and Shevtsov I. A. 1993.. Effect of antibiotics on the tissue culture of sugarbeet and fodder beet. Tsitologiya-i-Genetika 27(2): 3-6) used a combination of claforan and carbenicillin as inhibitors of Agrobacterium cells during transformation of diploid sugarbeet hybrid and 2 diploid varieties of fodder beet. However, the drawback of this report was that this combination had an inhibiting effect on shoot formation.

Yepes and Aldwinckle, 1994 (Yepes L. M. and Aldwinckle H. S. 1994.
Micropropagation of thirteen Mains cultivars and rootstocks, and effect of antibiotics
on proliferation. Plant Growth Regulation 15(1): 55-67) used cefotaxime at 200
mg/litre and carbenicillin at 500 mg/litre for the transformation of 13 apple cultivars.
However, the drawback of the report was that while cefatoxime caused abnormal
shoot morphology, carbenicillin alone or in combination with cefotaxime at 200
mg/litre, inhibited proliferation and caused excessive enlargement of the basal
leaves, inducing callus formation and release of phenolic compounds in the
medium.Linera/., 1995 (Lin-J J., Assad-GarciaN. andKuo, J. 1995.
Plant hormone effect of antibiotics on the transformation efficiency of plant tissues by
Agrobacterium tumefaciens cells. Plant Science Limerick. 109(2): 171-177) reported the
use of 250 to 2000 ug/ml carbenicillin for the inhibition of bacterial (A. tumefaciens
strains, LBA4404, C58 and EHA101) growth in tobacco leaf explants wherein they
showed that LBA4404 was the most sensitive to carbenicillin and cefotaxime. However,
the drawback of the protocol was that the regeneration efficiency from leaf explants
decreased with the addition of increasing concentration of carbenicillin on MS medium
containing 0.5 ug/ml of benzyladenine and/or 2,4-D wherein they emphasized on the
toxic effects on leaf explants when grown on MS medium containing a combination of
250 ug/ml carbenicillin and 1 ug/ml 2,4-D due to the auxin related chemical structures
of 2,4-D or NAA and carbenicillin. The major drawback of this protocol is that such
plant growth regulators (2,4-D, BA or NAA) are generally used in most regeneration
media that are employed for Agrobacterium tumefaciens mediated transformation.
Sarma et al., 1995 (Sarma K.S., Evans N.E. and Selby C. 1995. Effect of
carbenicillin and cefotaxime on somatic embryogenesis of Sitka spruce (Picea
sitchensis (Bong.) Carr. Journal of Experimental Botany 46(292):, 1779-81) reported
the use of antibiotics viz. carbenicillin and cefotaximethese in an attempt to transform
Sitka spruce somatic embryos using Agrobacterium based vectors. They reported that
carbenicillin should not be used for transformation of Sitka spruce. The drawback of
the report was that carbenicillin prevented the development of mature somatic
embryos, reduced early stage embryos by >90% and tissue growth by 50%.
Cefotaxime had no effect on overall tissue growth, but reduced the development of
early and mature embryos by 20% and 66-80%, respectively.
Shackelford and Chlan 1996 (Shackelfofd > Chlan C.A. 1996. Identification
of antibiotics that are effective in eliminating Agrobacterium tumefaciens. Plant

Molecular Biology Reporter 14(1): 50-5) performed an assay using ten antibiotics viz. cefotaxime, carbenicillin, tfrythromycin, spectinomycin, polymixin B, chloramphenicol, methicillin, augmentin 500, augmentin 250 and moxalactam [latamoxef] inorder to identify the antibiotics that are most effective against A. tumefaciens strains EHA101 and LBA4404, and to determine if these antibiotics inhibited tobacco callus and shoot formation. This report indicates that a major drawback of most transformation protocol is time consuming assays involving several costly antibiotics for the effective elimination of A. tumefaciens after gene transfer into plant explant has taken place.
Barrett et al., 1997 (Barrett C., Cobb E., McNicol.R. and Lyon G. 1997 A risk assessment study of plant genetic transformation using Agrobacterium and implications for analysis of transgenic plants. Plant Cell Tissue and Organ Culture. 47(2): 135-44) examined Agrobacterium transformation systems for Brassica, Solanum and Rubus, using carbenicillin, cefotaxime and ticaracillin [ticarcillin], respectively, to eliminate contamination, for the presence of residual Agrobacterium. Results indicated that none of the1 antibiotics tested succeeded in eliminating Agrobacterium and the contamination levels increased in explants from 12 to 16 weeks to such an extent that Solanum cultures senesced and died. This may be due to the fact that in some cases the minimum bactericidal concentration values (concentration to be used for elimination of contaminants in culture) for the three antibiotics were higher than the concentrations employed in the culture medium. Moreover, even up to 6 months after transformation, 50% of contaminated material still harboured bacterial cells with the binary vector at levels of 107 colony forming units per gram. This report indicates a major drawback with most of the generally used antibiotics are ineffective for Agrobacterium elimination in plants like Brassica, Solanum and Rubus and affects their regeneration as well as survival efficiency. Hammerschlag et al., 1997. (Hammerschlag F.A., Zimmerman R.H. Yadava, U.L., Hunsucker S. and Gercheva P. 1997. Effect of antibiotics and exposure to an acidified medium on the elimination of Agrobacterium tumefaciens from apple leaf explants and on shoot regeneration. Journal of the American Society for Horticultural Science. 122(6): 758-63) tested a range of antibiotics and their short-term exposure to an acidified (pH 3.0) medium for their effects on eliminating A. tu/t.^/aciens, supervirulent strain EHAld vp£HA101/pGT100), on leaf explam.. of Royal Gala apples (Malus domestica [M. pumila]) and on shoot regeneration.

They reported that the exposure of leaf explants to regeneration and elongation media containing 100 (ag/ml of the antibiotics carbenicillin (crb), cefotaxime (cef), and cefoxitin (mefoxin (mef)), singly or in combination for 52 days, did not eliminate A. tumefaciens from the explants. The drawback of this report was that even short-term (I to 18-hour) vacuum infiltration with 500 ^g/rnl of any of the antibiotics did not inhibit regeneration and failed to completely eliminate A. tumefaciens from leaf explants.
Cheng et al., 1998 (Cheng, Z. M., Schnurr, J. A. Kapaun, J. A. 1998.Timentin as an alternative antibiotic for suppression of Agrobacterium tumefaciens in genetic transformation. Plant Cell Reports 17(8): 646-9) studied the effects of timentin on shoot regeneration of tobacco (Nicotiana tabacum) and Siberian elm (Ulmus pumila) and its use for the suppression of Agrobacterium tumefaciens during genetic transformation. Timentinj - a mixture of ticarcillin and clavulanic acid was used effectively at concentrations of 200-500 mg/1 and at ratios of ticarcillinxlavulanic acid at 50:1 and 100:1. The drawback of this report is that although timentin is a less expensive alternative to the use of carbenicillin or cefotaxime antibiotics for the effective suppression of A. tumefaciens after genetic transformation yet it is expensive synthetic antibiotic as compared to natural agents like crude tea extracts. Ling et al., 1998 (Ling H.Q., Kriseleit D. and Ganal M.W. 1998. Effect of ticarcillin/potassium clavulanate on callus growth and shoot regeneration in Agrobacterium-mediated transformation of tomato (Lycopersicon esculentum Mill.) Plant Cell Reports 17(11): 843-7) studied the effect of Cefotaxime, ticarcillin/potassium clavulanate on tomato transformation. Cefotaxime did not inhibit callus growth in culture medium, but it clearly decreased shoot differentiation. While cefatoxime showed a strong negative effect on callus growth, shoot regeneration and transformation efficiency, the ticarcillin/potassium clavulanate was more economical and effective than carbenicillin and cefotaxime. The drawback of the report is that although ticarcillin/potassium clavulanate was a very good alternative to eliminate Agrobacteriurf tumefaciens in plant transformations yet it is an expensive synthetic antibiotic as compared to natural agents like crude tea extracts.
Joersbo et al. 2000 (Joersbo M., Brunstedt, J. Marcussen, J. Okkels FT. 2000. Transformation of the endospermous legume guar (Cyamopsis tetragonoloba L.) and analysis of transgene transmission. Molecular-Breeding 5(6): 521-9) used

carbenicillin and cefotaxime, for the elimination of Agrobacterium after co-culture, wherein they found considerable toxicity was displayed to guar tissues due to beta-lactams. When the beta-lactams were replaced by the non-phytotoxic beta-lactamase inhibitor usulbactam" alongwith thidiazuron and silver thiosulfate the problem was overcome. The drawback of this report was that while the commonly used carbenicillin and cefotaxime were phytotoxic to the explants used, replacement of beta-lactams by sulbactam is a costly process.
Objects of the present invention
The main object of the present invention is to develop a use of tea leaf extract for
killing the overgrowth of AgrobactaGum tumefaciens in systems or plants or explants
requiring longer co-cultivation periods in order to increase the transformation
efficiency.
Moreover, the crude tea extract is able to eliminate the risk of residual
Agrobacterium released along with the transgenic plants thereby maintaining a
balance between the selection pressures and the normal morphogenetic response.
Another object of the present invention is the use of tea leaf extract for
Agrobacterium tumefaciens genetic transformation in different systems or plants or
explants wherein rhe generally used bactericidal antibiotics are ineffective.
Further object of the present invention is to develop a use of tea leaf extract to
enhance the transformation efficacy of the bacteria Agrobacterium tumefaciens.
Another object of the present invention is to develop a use of tea leaf extract to
enhance prevent polyphenol oxidation involved with such kind of transformation.
Yet another object of the present invention is to develop use of tea leaf extract to
enhance wherein normal growth of the transformed plant is not affected by the this
mode of transformation involving bacteria Agrobacterium tumefaciens.
Yet another object of the present invention is to develop a cost-effective system for
Agrobacterium tumefaciens genetic transformation wherein no commercial and yet
costly antibiotics are used.
Still another object of the present invention is to develop an economical system for
obtaining the bactericidal agent without involving any costly extraction methods
wherein the crude leaf extract with bactericidal activity is extracted without requiring
expensive instruments.

Still another object of the invention is to develop a use of tea leaf extract wherein a
crude leaf extract with bactericidal activity can be obtained in abundance from
naturally growing tea bushes.
Still another object of the present invention is to develop a use of tea leaf extract
wherein the bactericidal agent is of natural origin and is not of synthetic or semi-
synthetic nature.
Still another object of present invention is to develop a use of tea leaf extract
wherein, the bactericidal agent can be obtained in abundance from actively growing
two and a bud making it economical.
Still another object of the present invention is to develop a use of tea leaf extract
t wherein, the bactericidal agent can be obtained in abundance from even the lower
maintenance foliage thereby making it more economical as generally such leaves are
discarded or burnt.
Still another object of the present invention is to develop a use of tea leaf extract
wherein, the crude leaf extract can also be used as a bactericidal agent for other
contaminating bacteria in different in vitro systems involving different plants or
explants.
Still another object of the present invention is to develop a use of tea leaf extract
wherein, the crude extract can also be used during 'hairy root production' using
Agrobacterium rhizogenesis. .
Still another object of the present invention is to develop use of tea leaf extract
wherein.the transformation efficiency can be increased considerably by decreasing
the mortality rate of transformants due to Agrobacterium overgrowth.
Further object of the present invention is to obtain tea leaf extract having bactericidal
property for Agrobacterium tumefaciens mediated genetic transformations which
obviates the drawbacks as detailed above.
Summary of the present invention
The present invention relates to an efficient and cost effective use of tea leaf extract
of preventing growth of genetic transformant bacteria Agrobacterium tumefaciens after transformation in plants by using tea leaf extract as a bactericide, wherein said use of tea leaf extract leads to elimination of common problem of polyphenol
oxidation during transformation and thereby he'^ maintain regeneration potential in
explan; ; and also helps in increased transforr efficacy.
Detailed description of the present invention
Accordingly, the present invention relates to an efficient and cost effective use of preventing growth of genetic transformant bacteria Agrobacterium tumefaciens after transformation in plants by using tea leaf extract as a bactericide, wherein said use leads to elimination of common problem of polyphenol oxidation during transformation and thereby helps maintain regeneration potential in explants and also helps in increased transformation efficacy.
«
In an embodiment of the present invention, use of tea leaf extract as a bactericide for
preventing growth of genetic •transformant bacteria Agrobacterium tumefaciens after
transformation in plants.
In another embodiment of the present invention, inoculating said bacteria harbouring
antibiotic resistant genes and reporter gus gene in a culture medium with said
antibiotics.
In yet another embodiment of the present invention, incubating the said culture in
dark.
In still another embodiment of the present invention, harvesting the ceils during log
phase
In still another embodiment of the present invention, pelleting live bacterial cells.
In still another embodiment of the present invention, suspending the said pellet in
fresh culture medium.
In still another embodiment of the present invention, optimizing the cells density.
In still another embodiment of the present invention, immersing various explants of
different plants in bacterial suspension.
In still another embodiment of the present invention, removing excess bacteria from
explant.
In still another embodiment of the present invention, incubating explant in media for
different time durations.
In still another embodiment of the present invention, preparing crude extract of tea
leaf to be used as bactericide by drying leaves.
In still another embodiment of the present invention, preparing acetone extract
overnight.
In • '!! another embodiment of the present ;nvention, filtering the extract.
In still another embodiment of the present invention, extracting filterate with n-hexane
to obtain aqueous and lipid layers.
In still another embodiment of the present invention, concentrating aqueous layer to
dryness.
In still another embodiment of the present invention, diluting concentrated extract
using with water to obtain crude tea extract.
In still another embodiment of the present invention, estimating total catechins and
caffeine in said extract.
In still another embodiment of the present invention, transferring explants of various
plants into medium containing various concentrations of 0-600 ug/ml of crude extract
(figure 1) and catechin and caffeine fractions separately.
In still another embodiment of the present invention, obtaining bacteria free
• transgenic explants.
4
In still another embodiment of the present invention, wherein antibiotics are selected
from a group comprising Kanamycin, and hygromycin.
In still another embodiment of the present invention, wherein culture medium is yeast
mannitol broth.
In still another embodiment of trto present invention, wherein concentration of
bacteria is ranging between 10.to 75 micrograms/ml.
In still another embodiment of the present invention, wherein incubating culture at
temperature ranging between 20 to 35° C.
In still another embodiment of the present invention, wherein incubating culture at
revolution rate ranging between 100 to 300 rpm for time duration ranging between 10
to 20 hours.
In still another embodiment "of the present invention, wherein harvesting the said
culture at optical density ranging between 0.6-0.8 at 600 nm for concentration of
about 1 x 109 cells/ml.
In still another embodiment of the present invention, wherein pelleting the harvest by
centrifuging at 3000-9000 rpm for about 20 to 40 minutes.
In still another embodiment of the present invention, wherein centrifuging said culture
at temperature ranging between 20 to 35° C.
In still another embodiment of the present invention, wherein cell density is measured
spectrophotometrically.
In still another embodiment of the present invention, wherein cell density is measured
by estimating optical density after about every 6 hours interval to estimate growth rate
of said bacteria spectrophotometrically.
In still another embodiment of the present invention, wherein optimization of cell
density has O.D. ranging between 0?6 to 0,8 at 600 nm at 1 X 109 cells/ml upto 60
hours.
In still another embodiment of the present invention, wherein immersing said tea
explant in bacterial suspension for time duration ranging between 3 to 40 minutes.
In still another embodiment of the present invention, wherein removing excess
bacteria from explant by blotting of explant on filter paper.
In still another embodiment of the present invention, wherein co-cultivating explant
for time duration ranging between 1 to 20 days.
•
In still another embodiment of the present invention, wherein concentration of tea
* plant extract is ranging between 1 to 1000 mlcrograms/ml.
In still another embodiment of the present invention, wherein leaves are dried in oven
\at temperature ranging between 50 to 70° C.
In still another embodiment of Jhe "present invention, wherein acetone is at
concentration ranging between 5 to 50 %.
In still another embodiment of the present invention, wherein acetone extract is
prepared at room temperature.
In still another embodiment of the present invention, wherein concentrating aqueous
layer to drying using rotary evaporators.
In still another embodiment of the present invention, wherein ratio of acetone and n-
hexane is ranging between 4:5 to 12:1.
In still another embodiment of the present invention, wherein concentration of tea leaf
•
extract in acetone solution is in the ratio ranging between 200 to 500 gms/L.
In still another embodiment of the present invention, wherein concentration of
catechins and caffeine is ranging between 2 to 750 micrograms/ml in culture.
In still another embodiment of the present invention, wherein using tea extract as
bactericide eliminates the problem of polyphenol oxidation.
In still another embodiment of the present invention, wherein said plants show normal
growth after using tea extract as bactericide.
In still another embodiment of the present invention, wherein said use of tea leaf
extract shows increased transformation efficacy.
In still another embodiment of the- present invention, whcrein.the transformation efficiency can be increased considerably- by decreasing the mortality rate of transformants due to Agrobacterium overgrowth.
In further embodiment of the present invention, the use of tea leaf extract of transformation used in the instant application employing bacteria Agrobacterium tumefaciens causes no polyphenol oxidation. The polyphenol oxidation usually affects the normal growth of the transformed plant in such kinds of transformation in plants. But, use of tea leaf extract as a bactericide after transformation of plant by said bacteria facilitate normal growth of the transformed plant. In another embodiment of the present invention, transformation efficacy facilitated by the said bacteria rises on the use of tea leaf extract as a bactericide for Agrobacterium tumefaciens. The said extract decreases the mortality rate of transformant due to bacterial overgrowth.
In further embodiment of the present Jinvention, tea leaf extract as a potent
bactericidal agent for Agrobacterium tumefaciens mediated genetic transformations
which comprises (i) inoculation of two strains of Agrobacterium tumefaciens viz.
EHA105 (mild) and GV2260 (virulent) harbouring the antibiotic resistance genes for
kanamycin or hygromycin and the reporter gus gene from mother cultures of
respective strains into 10-30 ml liquid modified Yeast Mannitol Broth with
kanamycin or hygromycin (ii) incubation for 12-16 hr at 25-30°C and 150-200 rpm
in dark (iii) harvesting at 0.6-0.8 optical density at 600 nm for lX109cells/ml during
log phase of bacterial growth (iv) pelleting of living bacterial cells by centrifugation
at 15-30 minutes at 4000-8000 rpm and 25-30°C (v) suspension of bacterial pellet in
fresh 5-25ml of Yeast Mannitol Broth without damaging the bacterial cells (vi)
optimization of bacterial cell density at lX109cells/ml by measuring optical density
at 600 nm (vii) immersion of various explants of different plants in bacterial
suspension for 5-35 minutes (viii) blotting of explants on filter papers to remove
excess Agrobacterium tumefaciens (ix) incubation of explants on incubation
medium for different periods of 1-10 days (x) preparation of crude
extract of tea leaf to be used as a bactericidal agent by drying 100-500g fresh tea
leaves of Kangra jat in an oven at 60°C (xi) overnight extraction of dried leaves at
room temperature with 0.4-1.2 liters of 10-40 ueous acetone and filteration (xii)
extraction of the filtrate with 100-500 ml nexane to obtain two layers for
removal of lipids (xiii) the aqueous layer taken and concentrated to dryness using
standard rotary evaporators (xiv) concentrated extract diluted with water to 10-50 ml and total catechins and caffeine estimated (xv) the aqueous extract served as a crude mixture (xvi) transfer of various explants of different plants to regeneration medium containing different concentrations of 0-600u.g/ml crude tea extract and catechin and caffeine fractions separately for totally killing the residual Agrobacterium tumefaciens and for eliminating the problem of polyphenol oxidation in the explants in order to maintain the regeneration potential of explants (xi) transfer of Agrobacterium tumefaciens free explants to regeneration medium containing selection antibiotics for further regeneration and transgenic plant development (xii) optimization of the concentration and fractions of tea leaf extract on the growth curve of Agrobacterium tumefaciens in both solid and liquid Yeast Mannitol Broth media in order to determine the optimum concentration for desired bactericidal activity as well as for promoting regeneration potential of the explant.
In further embodiment of the present invention, different explants of different plant species were used for transgenic production. In yet another embodiment of the present invention, different concentrations of filter
•
sterilized and autoclaved de-caffeinated fractions of catechin were added as above. In still another embodiment of the present invention, different concentrations of D-catechin of Acacia species were used as mentioned above wherein D-catechin was found to promote and not inhibit the growth of Agrobacterium tumefaciens. In still another embodiment of the present-invention, since green tea extract is known to have antimicrobial activity against several micro-organisms that are harmful to human health at minimum inhibitory concentration or MIC at 250|ig/ml to 1000u.g/ml, it was presumed that crude leaf extract could be used to kill overgrowing Agrobacterium tumefaciens during genetic transformation.
In still another embodiment of the present invention, this property of crude leaf extract can be successfully employed to overcome the serious problems of Agrobacterium tumefaciens overgrowth and also in preventing the loss of the transformants due to ineffective bactericidal antibiotics such as carbenicillin, cefatoxime, tricaricillin that are generally used in genetic transformation experiments in order to kill overgrowing Agrobacterium tumefaciens. Use of crude tea leaf extract for genetic transformation in plants not only has the potential of providing abundantly available natural source of bactericidal agent but is aiso
effective in cutting down the cost of commercially used antibiotics. Moreover, since the crude extracts are also obtained from the maintenance foliage leaves that are generally discarded and burnt, this use of tea leaf extract appears to be all the more economical and cost effective. Use of crude tea leaf extract is specially important in increasing the transformation efficiency because even the explants or plant species requiring long periods of co-cultivation can be recovered by killing the Agrobacterium tumefaciens.
In still another embodiment of the present invention, different explants like leaf, somatic embryo, callus and zygotic axes of tea were used using crude leaf extract of tea cultivars assamica and chinary instead "of generally used antibiotics for transgenic production following the use of tea leaf extract outlined in Example.
In still another embodiment of the present invention, different explants of different plant species like carnation and rose leaf, somatic embryo, callus were used during genetic transformation using crude leaf extract following the use of tea leaf extracts outlined in Example 1.
In still another embodiment of the present invention, different concentrations of filter sterilized and autoclaved de-caffeinated fractions of catechin were added as above for the production of transgenics instead of generally used antibiotics like carbenicillin, cefatoxime, tricaricillin etc. following the use of tea leaf extracts outlined in example 1. In still another embodiment of the present invention, different concentrations of D-catechin of Acacia species were used as mentioned above instead of generally used antibiotics like carbenicillin, cefatoxime, tricaricillin wherein D-catechin was found to promote and not inhibit the growth of Agrobacterium tumefaciens. In further embodiment of the present invention, applicant has claimed an extract as a potent bactericidal agent for Agrobacterium tumefaciens mediated genetic transformations comprising of steps (i) inoculation of two strains of Agrobacterium tumefaciens viz. EH A105 (mild) and GV2260 (virulent) harbouring the antibiotic resistance genes for kanamycin or hygromycin and the reporter gus gene from mother cultures of respective strains into 10-30 ml liquid modified Yeast Mannitol Broth with kanamycin or hygromycin (ii) incubation for 12-16 hr at 25-30°C and 150-200 rpm in dark (Hi) harvesting at 0.6-0.8 optical density at 600 nm for lX109cells/ml during log phase of bacterial growth (iv) pelleting of living bacterial cells by centrirugation at 15-30 minutes at 4000-8000 rpm and 25-30°C (v) suspension of bacterial pellet in fresh 5-25ml of Yeast Mannitol Broth without
damaging the bacterial cells (vi) optimization of bacterial cell density at lX109cells/ml by measuring optical density at 600 nm (vii) immersion of various explants of different plants in bacterial suspension for 5-35 minutes (viii) blotting of explants on filter papers to remove excess Agrobacterium tumefaciens (ix) incubation of explants on incubation medium for different periods of 1-10 days (x) preparation of crude extract of tea leaf to be used as a bactericidal agent by drying 100-500g fresh tea leaves of Kangra jat in an oven at 60°C (xi) overnight extraction of dried leaves at room temperature with 0.4-1.2 liters of 10-40% aqueous acetone and filteration (xii) extraction of the filtrate with 100-500 ml of n-hexane to obtain two layers for removal of lipids (xiii) the aqueous layer taken and concentrated to dryness using standard rotary evaporators (xiv) concentrated extract diluted with water to 10-50 ml and total catechins and caffeine estimated (xv) the aqueous extract served as a crude mixture (xvi) transfer of various explants of different plants to regeneration medium containing different concentrations of 0-600|ig/ml crude tea extract and catechin and caffeine fractions separately for totally killing the residual Agrobacterium tumefaciens and for eliminating the problem of polyphenol oxidation in the explants in order to maintain the regeneration potential of explants (xvii) transfer of Agrobacterium tumefaciens free explants to regeneration medium containing selection antibiotics for further regeneration and transgenic plant development (xviii) optimization of the concentration and fractions of tea leaf extract on the growth curve of Agrobacterium tumefaciens in both solid and liquid Yeast Mannitol Broth media in order to determine the optimum concentration for desired bactericidal activity as well as for promoting regeneration potential of the explant. In still another embodiment of the present invention, wherein two strains of Agrobacterium tumefaciens viz. EHA105 (mild) and GV2260 (virulent) harbouring the antibiotic resistance genes for kanamycin or hygromycin and the reporter gus gene from mother cultures of respective strains were inoculated into 10-30 ml liquid modified Yeast Mannitol Broth with "kanamycin or hygromycin. In still another embodiment of the present invention, wherein the above Agrobacterium tumefaciens cultures were harvested at 0.6-0.8 optical density at 600 nm for lX109cells/ml during log phase of bacterial growth.
In still another embodiment of the jjrtsent invention, wherein bacterial pellet was
suspended in fresh 5-25ml of Yeast Mannitol Broth without damaging the bacterial
cells.
In still another embodiment of the present invention, wherein bacterial cell density
was optimized at 1XI 09cells/ml by measuring optical density at 600 nm.
In still another embodiment of the present invention, wherein dried leaves overnight
extracted at room temperature with 0.4-1.2 liters of 10-40% aqueous acetone and
filtered and the filtrate extracted with 100-500 ml of n-hexane to obtain two layers
for removal of lipids.
In still another embodiment of the present invention, wherein concentrated extract
was diluted with water to 10-50 ml and total catechins and caffeine estimated.
In still another embodiment of the present invention, wherein the aqueous extract
served as a crude mixture.
In still another embodiment of the present invention, wherein various explants of
different plants were transferred to regeneration medium containing different
concentrations of 0-600ng/ml crude tea extract and catechin and caffeine fractions
separately for totally killing the .residual Agrobacterium tumefaciens and for
eliminating the problem of polyphenol oxidation in the explants in order to maintain
the regeneration potential of explants the cultures containing crude tea leaf extract
were maintained at 25-30°C.in dark at 150-200 rpm for 48 hr.
In still another embodiment of the present invention, wherein the crude leaf extract
having bactericidal properties can be obtained in abundance from even the lower
maintenance foliage thereby making it more economical as generally such leaves are
discarded or burnt.
In still another embodiment of the present invention, wherein the crude leaf extract
can also be used as a bactericidal agent for other contaminating bacteria in different
in vitro systems involving different plants or explants.
In still another embodiment of the present invention, wherein the crude leaf extract
can be used to increase the transformation efficiency considerably by decreasing the
mortality rate of transformants due to Agrobacterium overgrowth.
BRIEF DESCRIPTION OF THE ACCOMPANYING DRAWING
Fig.l shows spectrophotometric decrease in absorbance with increasing concentration of crude leaf extracts. The' concentration of crude leaf extract is ranging between l-400|ag/ml.
The following examples are given by way of illustration and therefore should not be
•
construed to limit the scope of the present jnvention.
EXAMPLE-1
Two strains of Agrobacterium tumefdctens viz. ERA 105 (mild) and GV2260
(virulent) harbouring the antibiotic resistance genes for kanamycin or hygromycin
**•• and the reporter gus gene were inoculated froni mother cultures of respective strains
into 10-30 ml liquid modified Yeast Mannitol Broth with kanamycin or hygromycin. The cultures were incubated for 12-16 hr at 25-30°C and 150-200 rpm in dark and harvested at 0.6-0.8 optical density at 600 nm for lX109cells/ml during log phase of bacterial growth. The living bacterial cells were pelleted by centrifugation at 15-30 minutes at 4000-8000 rpm and 25-30°C and suspended in fresh 5-25ml of Yeast Mannitol Broth without damaging the bacterial cells. The bacterial cell density at lX109cells/mi was optimized by measuring optical density at 600 nm.
Various explants of different plants were immersed in bacterial suspension for 5-35 minutes and blotted on filter papers to remove excess Agrobacterium tumefaciens. The explants were incubated on incubation medium for different periods of 1-10 days. Crude extract of tea leaf was prepared to be used as a bactericidal agent by drying 100-500g fresh tea leaves of Kangra jat in an oven at 60°C. Dried leaves were extracted overnight at room temperature with 0.4-1.2 liters of 10-40% aqueous acetone and filtered. The filtrate extracted with 100-500 ml of n-hexane to obtain two layers for removing lipids and the aqueous layer concentrated to dryness using standard rotary evaporators and diluted with water to 10-50 ml. Total catechins and caffeine estimated and the aqueous extract served as a crude mixture. Various explants of different plants were transferred to regeneration medium containing different concentrations of 0-600ng/ml crude tea extract for totally killing the residual Agrobacterium tumefaciens and for eliminating the pr, em of polyphenol oxidation in the e ints in order to maintain the regener >n potential of explants.
The Agrobacterium tumefaciew free 'explants were transferred to regeneration medium containing kanamycin or hygromycin for further regeneration and transgenic plant development. Concentrations and fractions of tea leaf extract were tested on the growth curve of Agrobacterium tumefaciens in both solid and liquid Yeast Mannitol Broth media in order to determine the optimum concentration for desired bactericidal activity as well as for promoting regeneration potential of the explant.
EXAMPLE-2
Two strains of Agrobacterium tumefaciens viz. EHA105 (mild) and GV2260
(virulent) harbouring the antibiotic resistance genes for kanamycin or hygromycin and the reporter gus gene were inoculated from mother cultures of respective strains into 10-30 ml liquid modified Yeast Mannitol Broth with kanamycin or hygromycin. The cultures were incubated for 12-16 hr at 25-30°C and 150-200 rpm in dark and harvested at 0.6-0.8 optical density at 600 nm for lX109cells/ml during log phase of bacterial growth. The living bacterial cells were pelleted by centrifugation at 15-30 minutes at 4000-J8000 rpm and 25-30°C and suspended in fresh 5-25ml of Yeast Mannitol Broth without damaging the bacterial cells. Measurement of optical density at 600 nm at regular 6hr intervals for 0-48 hr and the mean ot ihree readings were plotted for development of the growth curve. Crude mixture of catechins as well as caffeine at concentrations of 2-600ug/ml were added to fresh cultures of Agnobacterium tumefaciens and maintained at 25-30°C in dark at 150-200 rpm for 48 hr. The optical density was again measured at regular interval of 6 hr each for 0-48hr for the plotting of the mean of the three readings in a linear graph in order to determine the effect of the crude mixture of catechins as well as caffeine at concentrations of 2-600ng/ml on fresh cultures of Agrobacterium tumefaciens (Fig. 1).
EXAMPLE-3
Single colony of Agrobacterium tumefaciens was streaked on agar solidified plates
containing different concentrations 2-600jj,g/ml of crude tea leaf extract containing mixture of catechins and caffeine in order to determine its bactericidal effect on agar solidified media by incubating'the plates at 25-30°C in dark for 12-16 hr.
Advantages of the present invention:
1. The main advantage of the present invention is that its an efficient and cost
effective use of tea leaf extract of preventing growth of genetic transformant bacteria Agrobacteriwn tumefaciens after transformation in plants by using tea leaf extract as a bactericide.
2. Another advantage of the instant application is that it's a use of tea leaf extract
for enhanced genetic transformation in plant systems using bacteria
Agrobacterium tumefaciens as the transformant.
3. Yet another advantage of the present invention is that it's a use of tea leaf extract
for prevention of overgrowth of genetic transformant of plants wherein the
growth of the plant after transformation is normal with no polyphenol oxidation.
4. Still another advantage is a use of tea leaf extract wherein, crude tea leaf extract
can be used as a potent bactericidal agent for Agrobacterium tumefaciens
mediated genetic transformations as it can be used for killing the overgrowth of
Agrobacterium tumefaciens in systems or plants or explants requiring longer co-
cultivation periods thereby increasing the transformation efficiency.
5. Still another advantage is a use of tea 4eaf extract wherein, crude tea leaf extract
can be used for Agrobacterium tumefuCiens mediated genetic transformation in
different systems or plants or explants jvherein the generally used bactericidal
antibiotics are ineffective. v
6. Still another advantage is a use of tea leaf extract wherein, since no commercial
bactericidal antibiotics need to be used, crude tea leaf extract prove to be a cost
effective system for Agrobacterium tumefaciens mediated genetic transformation.
7. Still another advantage is a use of tea leaf extract wherein, since the crude leaf
extract with bactericidal activity is obtained without involving any expensive
instruments or costly extraction use of tea leaf extracts, its use proves to be an
economical use of tea leaf extract.
8. Still another advantage is a use of tea leaf extract wherein, the crude leaf extract
with bactericidal activity can be easily obtained in abundance from naturally
growing tea bushes round the year.
9. Still another advantage is a use of tea leaf extract wherein, the crude leaf extract
as a bactericidal agent is of natural origin and is not of synthetic or semi-
synthetic nature.

10. Still another advantage is a use of tea leaf extract wherein, the crude leaf extract
as a bactericidal agent can be obtained in abundance from even the lower
maintenance foliage thereby making it more economical as generally such leaves
are discarded or burnt.
11. Still another advantage is a use of tea leaf extract \vherein5 the crude leaf extract
can also be used as a bactericidal agent for other contaminating bacteria in
different in vitro systems involving different plants or explants.
12. Still another advantage is a use of tea leaf extract wherein, the crude tea leaf
extract can also be used during 'hairy root production' using Agrobacterium
rhizogenesis.
13. Still another advantage is a use of tea leaf extract wherein, the crude leaf extract
can be used to increase the transformation efficiency considerably by decreasing
the mortality rate of transformants due to Agrobacterium overgrowth.

We Claim:
1. A method of inhibiting growth of genetic transformant bacteria Agrobacterium tumefaciens after transformation in plants selected from the group consisting of tea, carnations, and roses, said method comprising: (1) inoculating Agrobacterium tumefaciens bacteria strains EHA105 and GV2260 harbouring antibiotic resistant genes for kanamycin and/or hygromycin and a reporter gus gene from mother cultures of said respective strains into a liquid-modified yeast mannitol broth with kanamycin and/or hygromycin, thereby forming a culture comprising said bacteria at a concentration of from 10 to 75 micrograms/ml; (2) incubating the culture in darkness for a time duration of 10 20 hours at a temperature of 20 35.degree. C. and at a revolution rate of 100 300 rpm; (3) after said incubation, harvesting the culture at 0.6 0.8 optical density at 600 nm for concentration of 1.times. lO.sup.9 cells/ml during log phase of bacterial growth; (4) pelleting live bacterial cells in the harvested culture by centrifuging the harvested culture for a time duration of 15 40 minutes at a revolution rate of 3000 9000 rpm and at a temperature of 20 35.degree. C, thereby forming a pellet; (5) suspending the pellet in a fresh yeast mannitol broth medium to form a bacterial suspension; (6) optimizing bacterial cell density at 1.times. lO.sup.9 cells/ml of the bacterial suspension by measuring optical density at 600 nm after about every 6 hours interval to estimate growth rate of the bacteria spectrophotometrically, wherein optimization of cell density has an optical density ranging between 0.6 and 0.8 at 600 nm at l.times. 10. sup. 9 cells/ml; (7) immersing one or more explants of one or more plants in the bacterial suspension for a time duration of from 3 to 40 minutes, the explants being selected from the group consisting of leaf, somatic embryo, callus and zygotic axes; (8) removing excess genetic transformant Agrobacterium tumefaciens bacteria from said one or more explants; (9) incubating the explants obtained in step (8) in an incubation medium for a time duration of from 1 to 20 days; (10) preparing a crude extract of tea by a process comprising: (a) drying fresh tea leaves of Kangra jat in an oven at a temperature of from 50.degree. C. to 700.degree. C; (b) combining the dried fresh tea leaves with a 10 40% aqueous acetone to form a leaves/acetone solution and subjecting said dried fresh tea leaves to overnight extraction at room temperature with the aqueous acetone to form an extract, the dried fresh leaves being present in the leaves/acetone solution at a concentration of from 200 to 500 grams/liter, and the acetone being present in the leaves/acetone solution at a concentration of from 5 to 50%; (c) filtering the extract to form a filtrate; (d) extracting the filtrate with n-hexane to obtain an aqueous layer and a lipid layer; the ratio of acetone or n-hexane during extraction being from 4:5 to 12:1; (e) concentrating the aqueous layer to dryness; and (f) diluting the concentrated aqueous layer with water to obtain said crude tea extract, the crude tea extract comprising catechins and caffeine at a concentration of from 2 to 750 micrograms/ml; (11) characterised in that the one or more explants as obtained in step (9) are transferred to a regeneration medium containing from 1 to 1000 micrograms/ml of the crude tea extract prepared in step (10); and (12) maintaining the one or more explants in said regeneration medium in darkness at 25 30.degree. C. at 150 200 rpm for 48 hours, thereby obtaining one or more explants upon which growth of genetic transformant bacteria Agrobacterium tumefaciens is inhibited.
2. A method as claimed in claim 1, wherein said tea extract eliminates polyphenol oxidation during transformation.

3. A method as claimed in claim 1, wherein said one or more explants show normal growth after incubation with said crude tea extract in step (12).
4.A method as claimed in claim 1, wherein cell density is measured spectrophotometrically.
5. A method as claimed in claim 1, wherein in step (8) said excess genetic transformant Agrobacterium tumefaciens bacteria is removed from said one or more explants by blotting said one or more explants on filter paper.
6. A method as claimed in claim 1, wherein in step (10)(a), the fresh tea leaves are dried in an oven at a temperature of 60.degree. C.
7. A method as claimed in claim 1, wherein in step (10)(e), said aqueous layer is concentrated to dryness using rotary evaporators.
8. A method as claimed in claim 1, wherein in step (2), said culture is incubated for a time duration of 12 16 hours at a temperature of 25 30.degree. C. and at a revolution rate of 150-200 rpm.
9. A method as claimed in claim 1, wherein in step (4), the harvest is pelleted by centrifuging at 4000 8000 rpm for a time duration of 15 to 30 minutes and at a temperature of 25-30.degree. C.

10. A method as claimed in claim 1, wherein said culture is centrifuged at a temperature ranging between 25 to 30.degree. C.
11. A method as claimed in claim 1, wherein in step (7), the one or more explants are immersed in the bacterial suspension for a time duration of from 5 to 35 minutes.
12. A method as claimed in claim 1, wherein in step (10)(b), the dried fresh tea leaves are combined with from 0.4 to 1.2 liters of the aqueous acetone.
13. A method as claimed in claim 1, wherein in step (10)(d), the filtrate is extracted with 100-500 ml of the n-hexane.
14. A method as claimed in claim 1, wherein in step (10)(f), the concentrated aqueous layer is diluted with water to 10-50 ml.

Documents:

2368-delnp-2004-abstract.pdf

2368-DELNP-2004-Claims-(15-10-2008).pdf

2368-delnp-2004-claims-(30-03-2009).pdf

2368-delnp-2004-claims.pdf

2368-delnp-2004-complete specification (granted).pdf

2368-DELNP-2004-Correspondence-Others-(15-10-2008).pdf

2368-delnp-2004-correspondence-others.pdf

2368-delnp-2004-description (complete).pdf

2368-delnp-2004-drawings.pdf

2368-delnp-2004-form-1.pdf

2368-delnp-2004-form-18.pdf

2368-delnp-2004-form-2.pdf

2368-DELNP-2004-Form-3-(15-10-2008).pdf

2368-delnp-2004-form-3.pdf

2368-delnp-2004-form-5.pdf

2368-DELNP-2004-Petition-137-(15-10-2008).pdf

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Patent Number

233570

Indian Patent Application Number

2368/DELNP/2004

PG Journal Number

14/2009

Publication Date

27-Mar-2009

Grant Date

30-Mar-2009

Date of Filing

13-Aug-2004

Name of Patentee

COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH

Applicant Address

RAFI MARG, NEW DELHI-110 001, INDIA.

Inventors:

#	Inventor's Name	Inventor's Address
1	ASHU GULATI	IHBT INDIA.
2	PARAMVIR SINGH AHUJA	IHBT INDIA.
3	INDRA SANDAL	IHBT INDIA.
4	AMITA BHATTACHARYA	IHBT INDIA.
5	SRIGIRIPURAM DESIKACHAR RAVINDRANATH	IHBT INDIA.

PCT International Classification Number

A61K 35/78

PCT International Application Number

PCT/IB02/01163

PCT International Filing date

2002-03-26

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	03826447.1	2005-11-11	U.S.A.
2	10/106,528	2002-03-27	U.S.A.
3	13019	2003-03-14	U.S.A.